Package 72162-2523-1

Brand: sotalol

Generic: sotalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2523-1
Digits Only 7216225231
Product NDC 72162-2523
Product ID 72162-2523_9d7f9a0e-6872-429c-b8b8-d458c045a6f2
Description

100 TABLET in 1 BOTTLE (72162-2523-1)

Marketing

Marketing Status
Marketed Since 2025-07-11
Brand sotalol
Generic sotalol hydrochloride
Sample Package No

Linked Drug Pages (1)

Sotalol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9d7f9a0e-6872-429c-b8b8-d458c045a6f2", "openfda": {"unii": ["HEC37C70XX"], "rxcui": ["1923424"], "spl_set_id": ["5962c4ee-c8f7-4e38-ab8c-4848c7644362"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2523-1)", "package_ndc": "72162-2523-1", "marketing_start_date": "20250711"}], "brand_name": "Sotalol", "product_id": "72162-2523_9d7f9a0e-6872-429c-b8b8-d458c045a6f2", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Antiarrhythmic [EPC]", "Cardiac Rhythm Alteration [PE]"], "product_ndc": "72162-2523", "generic_name": "Sotalol Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sotalol", "active_ingredients": [{"name": "SOTALOL HYDROCHLORIDE", "strength": "160 mg/1"}], "application_number": "ANDA207428", "marketing_category": "ANDA", "marketing_start_date": "20171206", "listing_expiration_date": "20261231"}